Improved Performance of Polymer Solar Cells by Thermal Evaporation of AgAl Alloy Nanostructures into the Hole-Transport Layer
Source abstract
Abstract
The performance characteristics of polymer solar cells (PSCs) incorporated with AgAl and Ag nanostructures and MoO 3 spacer layers were investigated. The power conversion efficiency (PCE) of PSCs is sensitive to the nominal thicknesses of the AgAl nanostructures and the MoO 3 spacer layer. The PCE of a PSC with a 3-nm-thick layer of AgAl nanostructures and a 1-nm-thick MoO 3 isolation layer reached 9.79%, which is higher than the PCE (8.55%) of the reference PSC without metal nanostructures. Compared to PSCs with Ag nanostructures, PSCs with AgAl nanostructures showed better stability and still retained 60% of their initial PCE values after aging for 120 days in air without encapsulation. The enhanced stability of the PSCs is attributed to the formation of AlO x, which can inhibit the diffusion of Ag atoms into the neighboring layer. The localized surface plasmonic resonance (LSPR) effect of AgAl nanostructures was retained by inserting an only 1-nm-thick MoO 3 spacer layer between the metal nanostructures and the metal electrode. Our work has demonstrated that using AgAl alloy instead of Ag as plasmonic nanostructures is a better strategy for improving the performance of PSCs, especially in terms of the stability of the cells.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Organic Light-Emitting Diodes Research · Thin-Film Transistor Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Engineering Research Center for Nanophotonics and Advanced Instrument, Ministry of Education, and School of Physics and Materials Science, East China Normal University, Shanghai 200062, China
School of Automation Engineering, Shanghai University of Electric Power, Shanghai 200090, China
Funding
National Natural Science Foundation of China
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